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Clinical Trial Summary

This is a randomized study between two accepted techniques of mesh fixation for laparoscopic hernia repair.


Clinical Trial Description

This is a randomized study in which subjects will undergo one or two currently accepted techniques of mesh fixation during laparoscopic ventral hernia repair. Subject will undergo mesh fixation with either trans-abdominal sutures and metallic tacks or metallic tacks only. Pain will be assessed through week 12, and hernia recurrence will be assessed for 2 years after surgery. Subjects will complete pain questionnaires at baseline, each day during hospital stay, and at follow-up visits at 2, 6, and 12 weeks after discharge. Quality of life questionnaires will be completed at baseline, at discharge from hospital, and during follow-up visits at 2, 6, and 12 weeks after discharge. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00905320
Study type Interventional
Source Indiana University
Contact
Status Completed
Phase N/A
Start date September 2009
Completion date November 21, 2018

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